ENST00000682338.1:c.1736A>T
|
ENSP00000507062.1:p.Tyr579Phe
|
|
ENST00000682793.1:c.1736A>T
|
ENSP00000506910.1:p.Tyr579Phe
|
|
ENST00000682838.1:c.*1478A>T
|
ENSP00000507652.1:n.*1478A>T
|
|
ENST00000683578.1:c.1736A>T
|
ENSP00000507430.1:p.Tyr579Phe
|
|
ENST00000683606.1:n.1342A>T
|
|
|
ENST00000683661.1:n.3271A>T
|
|
|
ENST00000684324.1:c.1736A>T
|
ENSP00000507937.1:p.Tyr579Phe
|
|
ENST00000684545.1:c.1736A>T
|
ENSP00000506733.1:p.Tyr579Phe
|
|
ENST00000684624.1:n.1113A>T
|
|
|
ENST00000684714.1:c.1707+29A>T
|
ENSP00000506861.1:n.1707+29A>T
|
|
ENST00000684731.1:n.1083+1341A>T
|
|
|
ENST00000375679.9:c.1736A>T
MANE Select
|
ENSP00000364831.5:p.Tyr579Phe
|
|
ENST00000375667.7:c.1229A>T
|
ENSP00000364819.3:p.Tyr410Phe
|
|
ENST00000375679.8:c.1736A>T
|
ENSP00000364831.4:p.Tyr579Phe
|
|
ENST00000431772.1:c.203A>T
|
ENSP00000389344.1:p.Tyr68Phe
|
|
ENST00000619181.4:c.1293+62A>T
|
ENSP00000483866.1:n.1293+62A>T
|
|
NM_000085.4:c.1736A>T
|
NP_000076.2:p.Tyr579Phe
|
|
NM_001165945.2:c.1229A>T
|
NP_001159417.2:p.Tyr410Phe
|
|
XM_011540619.1:c.1577A>T
|
XP_011538921.1:p.Tyr526Phe
|
|
XM_011540621.1:c.1085A>T
|
XP_011538923.1:p.Tyr362Phe
|
|
NM_000085.5:c.1736A>T
MANE Select
|
NP_000076.2:p.Tyr579Phe
|
|